Linked Data
ClinVar Variation Id:
215769
dbSNP Id:
rs779157605
ExAC:
3:10191559 C / T
gnomAD v2:
3-10191559-C-T
gnomAD v3:
3-10149875-C-T
gnomAD v4:
3-10149875-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10149875C>T , CM000665.2:g.10149875C>T | GRCh38 |
| NC_000003.11:g.10191559C>T , CM000665.1:g.10191559C>T | GRCh37 |
| NC_000003.10:g.10166559C>T | NCBI36 |
| NG_008212.3:g.13241C>T , LRG_322:g.13241C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.*229C>T | ENSP00000512434.1:n.*229C>T | |
| ENST00000696143.1:c.688C>T | ENSP00000512435.1:n.688C>T | |
| ENST00000696153.1:c.663C>T | ENSP00000512444.1:p.Leu221= | |
| ENST00000256474.3:c.552C>T MANE Select | ENSP00000256474.3:p.Leu184= | |
| ENST00000256474.2:c.552C>T | ENSP00000256474.2:p.Leu184= | |
| ENST00000345392.2:c.429C>T | ENSP00000344757.2:p.Leu143= | |
| ENST00000477538.1:n.688C>T | ||
| NM_000551.3:c.552C>T , LRG_322t1:c.552C>T | NP_000542.1:p.Leu184= | |
| NM_198156.2:c.429C>T | NP_937799.1:p.Leu143= | |
| NM_001354723.1:c.*106C>T | NP_001341652.1:n.*106C>T | |
| NM_000551.4:c.552C>T MANE Select | NP_000542.1:p.Leu184= | |
| NM_001354723.2:c.*106C>T | NP_001341652.1:n.*106C>T | |
| NM_198156.3:c.429C>T | NP_937799.1:p.Leu143= |